CTRI/2022/05/042810已完成4 期
A prospective, post market, non-interventional observational, open label, single arm, single center study to confirm clinical safety and performance of SkanRespiro Plus and Pranaa
试验速览
- 阶段
- 4 期
- 状态
- 已完成
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Adult and pediatric subjects of age more than two year or body weight of 10 kg above whichever is lower and of either gender.
- •Subjects who need mechanical ventilation.
- •Subject or the legally authorised representative on behalf of subject shall be capable of understanding and signing the informed consent form.
排除标准
- •Subjects with age less than two year or less than 10 kg of body weight.
- •Subjects who need ventilation during transport.
- •Pregnant or nursing mother.
- •Unconscious subjects shall be excluded from the non invasive mode of ventilation.
研究者
相似试验
已完成
4 期
Post Market Clinical Follow Up of Skanray s Patient MonitorsCTRI/2022/05/042811Skanray Technologies Limited
已完成
不适用
Post Market Clinical Follow Up Investigation of Intraskan DCCTRI/2020/12/029746Skanray Technologies Pvt Ltd
已完成
4 期
Post Market Clinical Follow Up Investigation of SKAN CCTRI/2020/12/029836Skanray Technologies Pvt Ltd
已完成
4 期
Post Market Clinical Follow Up Investigation of Skanmobile and Skanmobile DRCTRI/2020/09/028059Skanray Technologies Pvt Ltd
已完成
4 期
Post Market Clinical Follow Up Investigation of microSKACTRI/2020/12/029799Skanray Technologies Pvt Ltd
